# Biomedical Research & Development Laboratories, Inc.

- Location (FDA's records): Oklahoma City, OK
- FDA decisions: 3 (1984–1988): 3 510(k) clearances
- Product codes: LCX (1), JJR (1), JIX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K884693: Universal (TM) Ion Select Electrode Standards (Dec 15, 1988)
- K881655: Spectrum (TM) Blood Gas and Electrolyte Control (May 27, 1988)
- K834474: H.P.T. Home Preg. Test Kit & a.P.T. (Sep 28, 1984)

Source page: https://510kreport.com/company/biomedical-research-development-laboratories